Korf B R, Schuh B E, Salwen M J, Warburton D, Miller O J
Hum Genet. 1976 Jan 28;31(1):27-33. doi: 10.1007/BF00270396.
The role of trypsin in the elicitation of G-banding on human chromosomes was studied in two separate laboratories. Enzyme activity and ability of trypsin to chelate calcium were manipulated by dilution of the treatment solution, and by inhibition with diisopropylphosphofluoridate, diphenylcarbamyl chloride, or soybean trypsin inhibitor. In all cases, chromosomes were affected in proportion to the enzyme activity of the treatment solution rather than the ability of the solution to bind calcium. It is concluded that calcium chelation is not sufficient to explain G-banding trypsin, but that proteolytic activity is required.
在两个独立的实验室中研究了胰蛋白酶在人类染色体G显带诱导中的作用。通过稀释处理溶液以及用二异丙基氟磷酸酯、二苯基氨基甲酰氯或大豆胰蛋白酶抑制剂进行抑制,来控制胰蛋白酶的酶活性及其螯合钙的能力。在所有情况下,染色体受到的影响与处理溶液的酶活性成比例,而不是与溶液结合钙的能力成比例。得出的结论是,钙螯合不足以解释胰蛋白酶诱导的G显带,而是需要蛋白水解活性。